Publications

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Stacey, S. N., Sulem, P., Jonasdottir, A., Masson, G., Gudmundsson, J., Gudbjartsson, D. F., Magnusson, O. T., Gudjonsson, S. A., Sigurgeirsson, B., Thorisdottir, K., Ragnarsson, R., Benediktsdottir, K. R., Nexø, B. A., Tjønneland, A., Overvad, K., Rudnai, P., Gurzau, E., Koppova, K., Hemminki, K. ... Swedish Low-risk Colorectal Cancer Study Group (2011). A germline variant in the TP53 polyadenylation signal confers cancer susceptibility. Nature Genetics, 43(11), 1098-1103. https://doi.org/10.1038/ng.926
Steinberg, S., de Jong, S., Andreassen, O. A., Werge, T., Børglum, A. D., Mors, O., Mortensen, P. B., Gustafsson, O., Costas, J., Pietiläinen, O. P. H., Demontis, D., Papiol, S., Huttenlocher, J., Mattheisen, M., Breuer, R., Vassos, E., Giegling, I., Fraser, G., Walker, N. ... Irish Schizophrenia Genomics Consortium (2011). Common Variants at VRK2 and TCF4 Conferring Risk of Schizophrenia. Human Molecular Genetics, 20(20), 4076-81. https://doi.org/10.1093/hmg/ddr325
Steinberg, S., Mors, O., Børglum, A. D., Gustafsson, O., Werge, T., Mortensen, P. B., Andreassen, O. A., Sigurdsson, E., Thorgeirsson, T. E., Böttcher, Y., Olason, P., Ophoff, R. A., Cichon, S., Gudjonsdottir, I. H., Pietiläinen, O. P. H., Nyegaard, M., Tuulio-Henriksson, A., Ingason, A., Hansen, T. ... Genetic Risk and Outcome in Psychosis (2011). Expanding the range of ZNF804A variants conferring risk of psychosis. Molecular Psychiatry, 16(1), 59-66. https://doi.org/10.1038/mp.2009.149
Sunde, L. E. M., Niemann, I., Schmidt, B. & Bolund, L. (2011). Do all diploid HMs originate in triploid conceptuses?. Abstract from XVIth World Congress on Gestational Trophoblastic Diseases, Budapest, Hungary.
Tettelin, H. & Kilian, M. (2011). Genomes of Streptococcus mitis, Streptococcus oralis, and Streptococcus infantis. In P. E. Kolenbrander (Ed.), Oral Microbial Communities: Genomic Inquiry and Interspecies Communication (pp. 37-63). ASM Press.
Thomassen, M., Pedersen, I. S., Vogel, I., Hansen, T. V. O., Brasch-Andersen, C., Brasen, C. L., Crüger, D., Sunde, L., Nielsen, F. C., Jensen, U. B., Bisgaard, M. L., Borg, Å., Gerdes, A.-M. & Kruse, T. A. (2011). A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing. Breast Cancer Research and Treatment, 128 (1), 179-85. https://doi.org/10.1007/s10549-010-1272-6
Toyoshima, C., Kanai, R. & Cornelius, F. (2011). First crystal structure of Na+,K+-ATPase: New light on the oldest ion pump. Structure, 19, 1732-1738.